KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness (Q22008780)

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10 November 2019

title

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness (English)

1 reference

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Potassium voltage-gated channel subfamily Q member 4

10 November 2019

main subject

1 reference

GOA release 2020-03-11

potassium ion transport

1 reference

GOA release 2020-03-11

0 references

1 reference

1

C Kubisch

C

Kubisch

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10025409%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

5

A El-Amraoui

A

El-Amraoui

1 reference

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10 November 2019

7

C Petit

C

Petit

1 reference

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10 November 2019

8

T J Jentsch

T J

Jentsch

1 reference

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10 November 2019

B C Schroeder

2

B C

Schroeder

1 reference

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10 November 2019

T Friedrich

series ordinal

3

author given names

T

author last names

Friedrich

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10025409%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

B Lütjohann

series ordinal

4

author given names

B

author last names

Lütjohann

1 reference

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10 November 2019

S Marlin

series ordinal

6

author given names

S

author last names

Marlin

1 reference

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10 November 2019

language of work or name

English

0 references

publication date

1 February 1999

1 reference

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10 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10025409%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

volume

96

1 reference

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issue

3

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page(s)

437-446

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K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

10 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

A potassium channel mutation in neonatal human epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Connexin 26 gene linked to a dominant deafness.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Ionic currents of outer hair cells isolated from the guinea-pig cochlea

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Effects of salicylate and lanthanides on outer hair cell motility and associated gating charge

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

The fundamental and medical impacts of recent progress in research on hereditary hearing loss.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Heteromultimeric CLC chloride channels with novel properties

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Differential expression of outer hair cell potassium currents in the isolated cochlea of the guinea-pig

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

1 reference

7 January 2021

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

How well do we understand the cochlea?

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Genes responsible for human hereditary deafness: symphony of a thousand

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

KVLQT1 mutations in three families with familial or sporadic long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Cellular localization of rat Isk protein in the stria vascularis by immunohistochemical observation

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

The fine structure of spiral ligament cells relates to ion return to the stria and varies with place-frequency

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Evidence for a medial K+ recycling pathway from inner hair cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Mutations in the hminK gene cause long QT syndrome and suppress IKs function

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Cloning of a membrane protein that induces a slow voltage-gated potassium current

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Inner ear defects induced by null mutation of the isk gene

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Deafness in developing countries. Approaches to a global program of prevention.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980556-5

7 January 2021

10.1016/S0092-8674(00)80556-5

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

1335544

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10025409%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1335544

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

1335544